Journal
CHEMSUSCHEM
Volume 9, Issue 23, Pages 3353-3360Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.201601273
Keywords
carbon-oxygen bond cleavage; etherification; heterogeneous catalysis; hydrogen bond; lignin
Funding
- National Natural Science Foundation of China [91545102, 21473188, 21233008]
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Efficient depolymerization of woody biomass to produce natural phenolic alcohols not only preserves the original structure of lignin, but also makes the depolymerization process atom-efficient. Here, high yield production of natural phenolic alcohols (38.7 wt%) from woody biomass has been achieved using a Ni/C catalyst in a methanol-water co-solvent. The Ni-based catalyst can efficiently etherify the C-alpha-OH group in lignin beta-O-4 motifs under hydrogen atmosphere, which can break the hydrogen bond between the C-beta-O oxygen and the C-alpha-OH proton to facilitate the C-beta-O cleavage. It was reported that water can also accelerate the etherification of raw lignin with methanol through in situ formation of acid. Our results suggest that breaking the intramolecular hydrogen bonds can accelerate the C-beta-O cleavage, keeping the original structure of lignin unchanged. This work highlights the significance of structure modification in lignin depolymerization and displays a clear potential for the valorization of whole biomass.
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